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HRID 1033073作成日:2026年10月26日

Triethylamine → 4-[5-{3-(2-Acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazole

https://huagongshe.com/reaction/1033073

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物4-(5-Aminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazoleHCID 10399268—
反応物3-(Acetyloxy)propanoic acidHCID 12647151—
溶媒BenzeneHCID 241—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物4-[5-{3-(2-Acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazoleHCID 10021797—

反応手順

A mixture of 3-acetoxypropionic acid (2.5 g), diphenylphosphorylazide (4.3 ml) and triethylamine (2.6 ml) in dry benzene (50 ml) was stirred for an hour at 75° to 80° C. To the mixture was added to a mixture of 4-(5-aminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole (3.0 g) in a solution of tetrahydrofuran (45 ml) and methanol (45 ml) at ambient temperature, and the mixture was stirred for 2.5 hours at the same temperature. Evaporation of a solvent gave a residue, which was purified by column chromatography on silica gel eluting with a mixture of ethyl acetate and methanol (9:1, V/V). The eluted fractions containing the desired product were collected and evaporated in vacuo. The residue was recrystallized from a mixture of methanol, dioxane and isopropyl ether to give 4-[5-{3-(2-acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazole (1.82 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05308857
出典データセットuspto-grants-1994_05
ORD IDord-1e35ba9396e84701a89f6491da912058
出典メモuspto-grants-1994_05